Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion> ?p ?o ?g. }
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- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion type Assertion NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_head.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion description "[Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder caused by mutations in one of seven known genes (FANCA,C,D2,E,F,G and BRCA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion evidence source_evidence_literature NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion SIO_000772 14749703 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion wasDerivedFrom befree-20140225 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion wasGeneratedBy ECO_0000203 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.